Y. Takenaka et al., CRYSTALLINE-STATE RACEMIZATION OF A CHIRAL CYANOETHYL GROUP CONNECTEDBY A HYDROGEN-BOND, Acta crystallographica. Section B, Structural science, 49, 1993, pp. 272-277
The crystal of l]bis(dimethylgly-oximato)(pyrrolidine)cobalt(III) (dim
ethylglyoximato = 2,3-butanedione dioximato) revealed a gradual change
of cell parameters keeping the single-crystal form when it was irradi
ated by X-rays. It contains one water molecule as solvent in the asymm
etric unit. The reactive cyanoethyl group is hydrogen bonded to the wa
ter molecule. In spite of the restriction by the hydrogen bond, the or
dered chiral cyanoethyl group is converted to disordered racemates wit
hout degradation of crystallinity. The rate of the racemization can be
explained well by the cavity size of the cyanoethyl group.